- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00097305
Body-Oriented Therapy for Sexual Abuse Recovery
September 7, 2007 updated by: National Center for Complementary and Integrative Health (NCCIH)
Delving Intervention and Mindbody Integration
The purpose of this study is to examine and compare the effects of two body therapy approaches in women who have experienced child sexual abuse.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Women who have experienced child sexual abuse often display symptoms of dissociation and lack of bodily self-awareness which hinder the recovery process.
Mind-body researchers have examined alternative therapeutic approaches to eliminating these factors.
This study will compare a standardized therapeutic message to body-oriented therapy which involves a combination of hands-on bodywork and verbal therapy focused on somatic and emotional awareness.
Study Type
Interventional
Enrollment
24
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Washington
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Seattle, Washington, United States, 98195
- University of Washington School of Nursing
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
25 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Self-reported child sexual abuse
- In current psychotherapy for child sexual abuse recovery
Exclusion Criteria:
- Over 6 months of past experience with body-oriented therapy
- Diagnosis or medications for psychosis
- Drug or alcohol addiction
- Current abusive relationship
- Dissociative disorder
- In transition on psychotropic medication
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Cynthia Price, PhD, Assistant Professor, University of Washington School of Nursing
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Price, C. Characteristics of women seeking bodywork as an adjunct to psychotherapy during recovery from childhood sexual abuse. Journal of Bodywork and Movement Therapies, 8(1): 35-42, 2004.
- Price, C. Body-oriented therapy as an adjunct to psychotherapy in recovery from childhood abuse: A case study. Journal of Bodywork and Movement Therapies, 6(4): 228-236, 2002.
- Price C. Bodywork for childhood abuse treatment: a pilot-test comparison. 35th Annual Communicating Nursing Research Conference/16th Annual WIN Assembly, Health Disparities: Meeting the Challenge, April 18-20, 2002, Palm Springs, California. Communicating Nursing Research. 35(10):264, 2002.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2002
Study Registration Dates
First Submitted
November 19, 2004
First Submitted That Met QC Criteria
November 19, 2004
First Posted (Estimate)
November 22, 2004
Study Record Updates
Last Update Posted (Estimate)
September 11, 2007
Last Update Submitted That Met QC Criteria
September 7, 2007
Last Verified
August 1, 2006
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- F31AT001053 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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